ライフサイエンスコーパス: nonpermissive

1 missive for infection, while A172 cells were nonpermissive.

2 are present that make the local environment nonpermissive.

3 hile untransfected controls were essentially nonpermissive.

4 , progenitor cells, whereas neurons remained nonpermissive.

5 strain, including strains previously deemed nonpermissive.

6 that the failure of B19V DNA replication in nonpermissive 293 cells can be overcome by adenovirus in

7 nfection under permissive (33 degrees C) and nonpermissive (37 degrees C) temperatures.

8 hromosome (BAC) transgenic line expressing a nonpermissive allele of Naip5 exhibits a reduction in ma

9 imary LCs harvested from mouse epidermis was nonpermissive, although a viral reporter protein was exp

10 In the lungs of nonpermissive BALB/c mice, L. pneumophila does not repli

11 Dot/Icm-dependent activation of caspase-1 in nonpermissive BALB/c mouse-derived macrophages, caspase-

12 s in antiviral signaling, but a minority are nonpermissive because the virus infection aborts before

13 e generated new cdc13-ts reagents, which are nonpermissive below 34 degrees , to allow examination of

14 but resides in a low molecular mass form in nonpermissive, blood-derived naive CD4 T cells.

15 ncorporating [(35)S]methionine into Atp8p at nonpermissive but not at the permissive temperature.

16 tes and several leukemic T-cell lines termed nonpermissive, but not in other cells termed permissive.

17 an unopposed innate response in replication-nonpermissive bystander cells.

18 it(+) cardiac progenitors and suggest that a nonpermissive cardiac milieu, rather than minimal cardio

19 d how abortive infection of resting and thus nonpermissive CD4 T cells in lymphoid tissues triggers a

20 A549), one semi-permissive (786-0), and one nonpermissive cell line (PANC-1).

21 runcated and chimeric forms of fJAM-A into a nonpermissive cell line and assayed binding by flow cyto

22 y to infect and replicate in this previously nonpermissive cell line.

23 the protein synthesis profile in previously nonpermissive cell lines, as well as early U(S)11 transc

24 he permissive cell functions required by the nonpermissive cell to ensure infectious virus production

25 HSV-1), is required for viral replication in nonpermissive cell types and for expression of a class o

26 us envelope gene allowing virus entry into a nonpermissive cell.

27 t were not explainable by a failure to enter nonpermissive cells and were not complemented in an ICP2

28 increased B19V capsid protein production in nonpermissive cells by codon optimization.

29 ike particles were successfully generated in nonpermissive cells by transient transfection of a plasm

30 a JAM-A mutant lacking a cytoplasmic tail in nonpermissive cells conferred full susceptibility to reo

31 ry (CHO) cells are traditionally regarded as nonpermissive cells for herpes simplex virus type 1 (HSV

32 leaved internal scaffold, were purified from nonpermissive cells infected with UL17, UL25, or UL6 nul

33 Expression of the feline SLC35F2 cDNA in nonpermissive cells renders the cells susceptible to inf

34 -1 integrase mutant replication in otherwise nonpermissive cells suggests alternative approaches to s

35 ut was not mutated in permissive cells or in nonpermissive cells that block secondary viral spread.

36 ol transporter 1 (mSMIT1) allowed previously nonpermissive cells to be infected by HEMV, indicating t

37 RhoC protein in EBOV and VSV permissive and nonpermissive cells were consistent with the cDNA gene a

38 Transfection of nonpermissive cells with alphav or beta1 cDNAs confers h

39 By infecting nonpermissive cells with this library and screening for

40 ary blood lymphocytes, certain T-cell lines (nonpermissive cells), and most likely in vivo is highly

41 We show that syndecan, when expressed in nonpermissive cells, becomes the major mediator for HIV

42 ceptibility to FeLV-A when reintroduced into nonpermissive cells, but it did not render these cells p

43 orced by heterologous replication systems in nonpermissive cells, enhanced readthrough of (pA)p and t

44 r fusion on HCMV-permissive cells but not on nonpermissive cells.

45 V)-permissive phenotype when introduced into nonpermissive cells.

46 n and integration appear to be unimpaired in nonpermissive cells.

47 other parvoviruses inhibit proliferation of nonpermissive cells.

48 sufficient to mediate viral entry into ALV-J nonpermissive cells.

49 a key factor in capsid protein production in nonpermissive cells.

50 Vif protein are replication incompetent in 'nonpermissive' cells, such as primary T cells and the T-

51 n cDNA, along with a cDNA encoding JAM-A, in nonpermissive chicken embryo fibroblasts conferred susce

52 directed pathogenic hantavirus infection of nonpermissive CHO cells expressing chimeric alphavbeta3

53 These repressive effects of nonpermissive chromatin cannot be completely countered b

54 Moreover, nonpermissive chromatin progressively silences a transge

55 K4 methylation at a transgenic promoter in a nonpermissive chromatin region are stochastic, leading t

56 thyl-H3-K9 ratio to that characteristic of a nonpermissive chromatin state.

57 edicated loci but also promotes shaping of a nonpermissive chromatin through its capacity to recruit

58 ontrast to HIV-1 permissive clone 10 (plus), nonpermissive clone 17 (minus) was adherent to coverslip

59 cell-surface HLE expression on HLE null, HIV nonpermissive clones permits HIV infectivity.

60 to granules, but not the cell surface of HIV nonpermissive clones.

61 differentiation in liquid medium, a normally nonpermissive condition.

62 lows growth of the E. coli fabG strain under nonpermissive conditions and restores in vitro fatty aci

63 of each unsuppressed mutant to divide under nonpermissive conditions correlated with the presence of

64 ene transcript levels between permissive and nonpermissive conditions for E. chaffeensis growth.

65 Growth of Lud135 under nonpermissive conditions is restored by the presence of

66 wever, possible low-level L2 synthesis under nonpermissive conditions led to ambiguity in interpretat

67 A:dT) tract-stimulated gene expression under nonpermissive conditions led to shifts of positioned nuc

68 ion, B104-5 cells with a dispersed ERC under nonpermissive conditions were more resistant to cisplati

69 ssive conditions, permissive conditions, and nonpermissive conditions with wild-type EBNA3C transcomp

70 However, under nonpermissive conditions, all stages of virus morphogene

71 At nonpermissive conditions, although trafficking of secret

72 s in DNA replication and morphogenesis under nonpermissive conditions, depending upon the experimenta

73 membrane proteins appeared unaffected under nonpermissive conditions, distinguishing the phenotype o

74 and pta rec mutants are not killed under the nonpermissive conditions, exemplifying a case of synthet

75 After shift to nonpermissive conditions, however, ten1-ts mutants accum

76 though the L2 protein was not detected under nonpermissive conditions, minute amounts could account f

77 Under nonpermissive conditions, morphogenesis was blocked and

78 ll wall compared with wild-type plants under nonpermissive conditions, no indications were found for

79 Under nonpermissive conditions, our conditional mutants of YNL

80 NAs were assayed for each EBNA3CHT LCL under nonpermissive conditions, permissive conditions, and non

81 is known to exhibit a runaway cell death in nonpermissive conditions, proves to be more tolerant to

82 Under nonpermissive conditions, spindles in td-kip3 doc1Delta

83 onditional effect on root architecture under nonpermissive conditions, suggesting they are also diffe

84 the LCLs specifically sustained growth under nonpermissive conditions, whereas EBNA3B or EBNA3C expre

85 complementation with EBNA3C for growth under nonpermissive conditions.

86 chaperonin, GroEL, helps proteins fold under nonpermissive conditions.

87 DNA replication occurs in these cells under nonpermissive conditions.

88 vision block seen in all shape mutants under nonpermissive conditions.

89 egmatis 628-53 undergoes filamentation under nonpermissive conditions.

90 oth dnaE and Deltathy mutants filament under nonpermissive conditions.

91 on, was synthesized by the G5R mutants under nonpermissive conditions.

92 ctive internal structures are produced under nonpermissive conditions.

93 ition to being a swarming cue under normally nonpermissive conditions.

94 due to depletion of the mutant protein under nonpermissive conditions.

95 low slow growth of pta recBC(Ts) cells under nonpermissive conditions; all three are in or near genes

96 ated protein folding were carried out under "nonpermissive" conditions, where the chaperonin system w

97 While U2AF(59) inactivation (nonpermissive) conditions inhibit splicing of some intro

98 Phenotypic analysis of nonpermissive Cts11 infections indicated that these amin

99 ants to sustain ongoing DNA synthesis during nonpermissive Cts24 infections, only a wtD5 allele suppo

100 sed to recombinant TGF-beta1 (or TGF-beta2), nonpermissive culture podocytes switch to G2/M arrest an

101 duces G0/G1 arrest and differentiation under nonpermissive culture through Smad3-dependent induction

102 er via exosomes drives antiviral immunity in nonpermissive DCs.

103 In contrast, a nonpermissive dimethyl-H3-K4/dimethyl-H3-K9 chromatin st

104 his issue of Blood, Pidala et al report that nonpermissive DPB1 allele mismatch is associated with in

105 1 also prevented AcMNPV-induced apoptosis in nonpermissive Drosophila melanogaster cells.

106 ailure of these integrins to be activated on nonpermissive ECM is because of active suppression by th

107 elongation is principally attributed to the nonpermissive environment and reduced intrinsic growth c

108 of the reduced intrinsic growth capacity and nonpermissive environment for axonal elongation.

109 factors and underexpress others, creating a nonpermissive environment for cocultured motor neurons.

110 These metabolic shifts created a nonpermissive environment for the Enterobacteriaceae rec

111 cumulate at demyelinating lesions creating a nonpermissive environment that impairs axon regeneration

112 o direct cell autonomous growth even in this nonpermissive environment.

113 These results suggest that nonpermissive expression of RUNX3 protein is restricted

114 characterized 43 cell lines as permissive or nonpermissive for AAV-5 transduction and compared the ge

115 o at pH 5.2 and also at pH 6.8, a pH that is nonpermissive for assembly of L1 protein alone.

116 vored in cells which are both permissive and nonpermissive for B19 viral replication.

117 Hepatocytes are nonpermissive for B19 virus replication.

118 tified a human cell line (HeLa-USU) that was nonpermissive for fusion and virus infection.

119 n, were expressed in the cytoplasm, and were nonpermissive for HCV infection.

120 te differentiation into macrophages that are nonpermissive for HIV-1 infection.

121 In resting CD4(+) T cells which are nonpermissive for HIV-1 replication, the levels of Cycli

122 viral translation under conditions that are nonpermissive for host cell translation.

123 ied under conditions that are permissive and nonpermissive for hr1.

124 ired for viral replication in cells that are nonpermissive for ICP22 mutants.

125 most cell lines and primary human cells are nonpermissive for integrase mutant growth.

126 crophages from most inbred mouse strains are nonpermissive for intracellular replication and allow li

127 Dendritic cells from both strains were nonpermissive for L. pneumophila intracellular growth, s

128 al forebrain regions neighboring the MGE are nonpermissive for MGE cell migration, whereas the dorsal

129 Although the normal host microenvironment is nonpermissive for neoplastic progression, tumor-reactive

130 s of the RNA polymerase beta' subunit and is nonpermissive for plating of bacteriophage P2.

131 ve infection with HSV-2 but were selectively nonpermissive for productive infection with HSV-1, a phe

132 t the nonpermissive neuronal subtype is also nonpermissive for reactivation.

133 ell receptor ligation in conditions that are nonpermissive for replication.

134 er proteins (Yops) under conditions that are nonpermissive for synthesis and secretion in wild-type s

135 gered by depolarization of the membrane were nonpermissive for the hybrid endolysin, indicating that

136 nes distinct chromatin regions permissive or nonpermissive for transgene expression.

137 Xrn1 KO A549 cells were viable but nonpermissive for VACV; however, wild-type and mutant vi

138 ivity and suggest a means to render the host nonpermissive for viral replication.

139 se bacteriophages to plaque on the otherwise nonpermissive groES or groEL mutant hosts in an allele-s

140 NiV infection-permissive cells but not to a nonpermissive HeLa cell line clone, suggesting that it b

141 esis at 34 degrees C in permissive (BHK) and nonpermissive (HEp-2) cells, but D1671V reduced in vitro

142 ought to be incapable of ligand binding in a nonpermissive heterodimer, such as that of thyroid hormo

143 plit segment were impaired in replication at nonpermissive high temperatures, whereas high viral tite

144 Nonpermissive HLA-DPB1 allele mismatch was associated wi

145 related donor HCT survival, and avoidance of nonpermissive HLA-DPB1 mismatches in otherwise HLA-match

146 ovel concept of DeltaFD sheds new light onto nonpermissive HLA-DPB1 mismatches in unrelated HCT.

147 Here, we investigated this question in nonpermissive HLA-DPB1 T-cell epitope (TCE) mismatches r

148 ive hosts of its parental viruses but also a nonpermissive host (Spodoptera litura).

149 within macrophages and tissues from mice, a nonpermissive host.

150 When introduced into nonpermissive human 293T cells and quail QT6 cells, chNH

151 and APOBEC3G are extensively coexpressed in nonpermissive human cells, including primary lymphocytes

152 ression of the putative HCV receptor CD81 on nonpermissive human hepatic but not murine cells enabled

153 ns, resulting in abortive HIV replication in nonpermissive human T cells.

154 e vectors for permissive (i.e., poultry) and nonpermissive (i.e., mammals, including humans) species,

155 lded efficient replication in Tag-expressing nonpermissive Jurkat T cells without reversion to an int

156 ypes, such as production of cholera toxin in nonpermissive LB medium, reduced resistance to high osmo

157 Nonpermissive ligands indirectly inhibited TCR binding b

158 arrying foreign Ags, permissive ligands, and nonpermissive lipid ligands clarifies the molecular basi

159 GP1 fragment nor that of ebolavirus bound a nonpermissive lymphocyte cell line.

160 We isolated a BVDV-nonpermissive MDBK cell clone that harbored a 1.2-kb ins

161 y to promote swarming when added to normally nonpermissive media.

162 the most sensitive, showing rapid killing in nonpermissive medium.

163 ch that allowed the immune reconstitution of nonpermissive mice following injection of human hematopo

164 from myeloma-permissive mice, into otherwise nonpermissive mice resulted in myeloma development, asso

165 cue entry into an undifferentiated, normally nonpermissive monocytic cell line.

166 onitis virus (FIPV) WSU 79-1146 and DF2 into nonpermissive mouse 3T3 cells can be rescued by the expr

167 into mouse fibroblasts allowed the normally nonpermissive mouse cells to become productively infecte

168 activation of caspase 1 and pyropoptosis in nonpermissive mouse macrophages.

169 ther caspase-3 is activated in permissive or nonpermissive mouse macrophages.

170 opism of HSV1716 was also evident in another nonpermissive mouse melanoma cell line and is an exclusi

171 In AWT experiments employing the nonpermissive murine model, C57BL/6 mice given adult wor

172 Here we show that HCMV transiently protects nonpermissive myeloid cells from chemical and virus entr

173 ing CSPG and control substrata confirmed the nonpermissive nature of CSPGs for OPC adhesion and morph

174 om non-A5(+) neurons, demonstrating that the nonpermissive neuronal subtype is also nonpermissive for

175 ulibacter in cells from permissive (CGD) and nonpermissive (normal) hosts and identifies potentially

176 feature is that the permissive cells, unlike nonpermissive ones, have ceased to proliferate in vivo a

177 Macrophage/microglia formed a nonpermissive OV barrier, preventing dissemination of oH

178 by the Lgn1 gene locus, which expresses the nonpermissive phenotype in cells from BALB/c mice but th

179 ive activation of the enzyme under otherwise nonpermissive physiological redox potentials.

180 ependent compensatory interferon response in nonpermissive plasmacytoid dendritic cells (pDCs).

181 MT and ST in both permissive mouse cells and nonpermissive rat cells.

182 3 K4 methylation and H3 acetylation, while a nonpermissive region is poor in or depleted of these two

183 epulsive interactions between the kinase and nonpermissive residue(s).

184 ification of sequence contextual effects and nonpermissive residues.

185 arcoma virus (RSV) genome association with a nonpermissive rodent host cell genome.

186 ion acts as a barrier to infection for other nonpermissive small-animal species, namely, ferret, guin

187 We demonstrate that the nonpermissive state exhibited by the majority of resting

188 d normally permissive CEMss cells to adopt a nonpermissive state, able to resist an HIV-1Deltavif cha

189 d long-term SSC cultures were derived from a nonpermissive strain that showed limited self-renewal di

190 ost inbred strains, as well as a variant for nonpermissive strains.

191 These results identify CSPGs as a nonpermissive substrate for OPCs and oligodendrocytes, a

192 osed by the spatiotemporal distribution of a nonpermissive substrate provided by versican, an extrace

193 accelerates axon growth over permissive and nonpermissive substrates, including major CNS inhibitors

194 markedly facilitates axon regeneration over nonpermissive substrates.

195 (HIV-1/Delta vif) from an acute infection of nonpermissive T cells and performed a thorough examinati

196 efficient gene expression and replication in nonpermissive T-cell lines and primary cells.

197 showed a significantly higher percentage of nonpermissive TCE mismatches for DeltaFD >2.665, compare

198 Although dhc1b-3 flagella at the nonpermissive temperature (34 degrees C) showed a dramat

199 When shifted to the nonpermissive temperature (37 degrees C), TRF2ts cells s

200 tential at 33 degrees C, but on shift to the nonpermissive temperature (39 degrees C), they show dimi

201 y synthesized lipid A was not cleaved at the nonpermissive temperature (44 degrees C).

202 At the nonpermissive temperature (NPT), tsB7 capsids accumulate

203 roduced immediate-early (IE) proteins at the nonpermissive temperature (NPT).

204 Dts38], Dts12, and Dts56) and shown that at nonpermissive temperature all of the tsD5 viruses exhibi

205 Incubation at the nonpermissive temperature also precluded coimmunoprecipi

206 Ad2ts1 was prepared at a nonpermissive temperature and contains the precursor for

207 mutations was inhibited upon a shift to the nonpermissive temperature and in the latter case decline

208 a temperature-sensitive VSV-M mutant at the nonpermissive temperature both substantially reversed th

209 M failed to accumulate in the nucleus at the nonpermissive temperature but did accumulate when the pe

210 e temperature and after several hours at the nonpermissive temperature but display aberrant organizat

211 Apoptosis also was suppressed at the nonpermissive temperature by constitutively active Akt a

212 e protected from cell death on incubation at nonpermissive temperature by mutation in the cydA gene c

213 synthesis, and thus lack of function at the nonpermissive temperature cannot be attributed to a lack

214 plasm of cells that had been infected at the nonpermissive temperature contained large granular areas

215 strong mouse-specific defect of PV1(RIPO) at nonpermissive temperature correlated with the translatio

216 Virions produced at the nonpermissive temperature do not assemble capsids, altho

217 cdc5-1 mutants arrest at telophase at the nonpermissive temperature due to the failure of CDK inac

218 e mutant proteins were largely stable at the nonpermissive temperature except the A68T/N73D mutant pr

219 cantly reduced if assayed at 30 degrees C, a nonpermissive temperature for Ty1 retrotransposition, or

220 This transcript is also absent at nonpermissive temperature in a 10-1 mouse cell line lack

221 risingly, certain ftsZ84 strains lyse at the nonpermissive temperature instead of filamenting, and in

222 infection is initiated and maintained at the nonpermissive temperature of 39.5 degrees C.

223 After a shift to the nonpermissive temperature of 40.5 degrees C, the rates o

224 ibits a loss of silencing when raised to the nonpermissive temperature regardless of cell-cycle posit

225 Passage of tsS133A and tsF219L at the nonpermissive temperature resulted in emergence of multi

226 xamination of ts1249 capsids produced at the nonpermissive temperature revealed that, in comparison w

227 s of tsE NSP2 were significantly less at the nonpermissive temperature than at the permissive tempera

228 rat8-2p localized to cytoplasmic granules at nonpermissive temperature that are distinct from P-bodie

229 We demonstrated that at the nonpermissive temperature the DnaB(A116V) mutant arreste

230 At the nonpermissive temperature these mutations have drastic e

231 cdc13-1 yeast grown at the nonpermissive temperature undergo G2/M arrest, progressi

232 shown that these cells enter mitosis at the nonpermissive temperature upon incubation with okadaic a

233 Overexpression of topoisomerase III at the nonpermissive temperature was shown subsequently to rest

234 her (i) a temperature-sensitive virus at its nonpermissive temperature which does not inject viral DN

235 ressors of dnaN5 that restored growth at the nonpermissive temperature while maintaining an increase

236 s mutant ceased after one cell doubling at a nonpermissive temperature, 37 degrees C.

237 120/R273K mutant suppressed apoptosis at the nonpermissive temperature, a phenotype correlated with i

238 Upon a shift to a nonpermissive temperature, both large and small-ribosoma

239 At nonpermissive temperature, bub3 clb5-ts cells showed def

240 ouble-mutant phenotype indicated that at the nonpermissive temperature, cells failed to undergo cytok

241 or olsA gene products supported growth at a nonpermissive temperature, exhibited AGPAT activity in v

242 lication immediately halts upon a shift to a nonpermissive temperature, growth and DNA replication of

243 archaeal and bacterial cysS genes grew at a nonpermissive temperature, growth was also supported by

244 hibited upon shift of mutant cultures to the nonpermissive temperature, indicating blockage of the sy

245 1% at the permissive temperature, and at the nonpermissive temperature, it renders further deteriorat

246 in virus-infected cells showed that, at the nonpermissive temperature, MHV-Brtsc31 was not able to p

247 of temperature-sensitive E. coli Y815 at the nonpermissive temperature, supporting its biological act

248 At the nonpermissive temperature, the capsids accumulate at the

249 At the nonpermissive temperature, this virus, designated ts8-22

250 At the nonpermissive temperature, vA6L-mut2 was normal at viral

251 At the nonpermissive temperature, viral gene expression and DNA

252 cause thermolability of the protein; at the nonpermissive temperature, virion morphogenesis arrests

253 pendent leader peptidase is inhibited at the nonpermissive temperature, whereas the insertion of the

254 e yip1-4 allele accumulate ER membranes at a nonpermissive temperature, with no apparent accumulation

255 ts showed reduced nuclear proteasomes at the nonpermissive temperature.

256 ented E. coli strain sensitive to GFZ at the nonpermissive temperature.

257 partial restoration of nsp5 activity at the nonpermissive temperature.

258 host cell but had an uncoating defect at the nonpermissive temperature.

259 dentical to that of Alb/ts/nsp5/V148A at the nonpermissive temperature.

260 d fewer myxospores than the wild type at the nonpermissive temperature.

261 is mutant also fails to enter S phase at the nonpermissive temperature.

262 pro, blocking its function completely at the nonpermissive temperature.

263 5 with the U(L)28 and U(L)33 proteins at the nonpermissive temperature.

264 m10 in mcm10-1 mutants that are grown at the nonpermissive temperature.

265 nts after 24 h of incubation in LB medium at nonpermissive temperature.

266 ants, even after prolonged incubation at the nonpermissive temperature.

267 ally assumes that the protein is inactive at nonpermissive temperature.

268 mutant FabG proteins may be disrupted at the nonpermissive temperature.

269 in mutant, and the VSV-G ts045 mutant at the nonpermissive temperature.

270 rain JN394top2-4 expressing betaE522K at the nonpermissive temperature.

271 ured in vivo was inhibited upon shift to the nonpermissive temperature.

272 undergo rapid apoptosis after a shift to the nonpermissive temperature.

273 ject its virion DNA into the nucleus at this nonpermissive temperature.

274 islocalized to the vacuole in neo1-ts at the nonpermissive temperature.

275 he viral life cycle that was affected at the nonpermissive temperature.

276 n mutant cells before and after the shift to nonpermissive temperature.

277 erature-sensitive mutant when shifted to the nonpermissive temperature.

278 2 viral DNA replication is unimpaired at the nonpermissive temperature.

279 ast-acting mei-1(ts) mutant was shifted to a nonpermissive temperature.

280 nsp5-mediated polyprotein processing at the nonpermissive temperature.

281 MHV-Brts31-infected cells is reduced at the nonpermissive temperature.

282 The transfer of endothelial cells to nonpermissive temperatures (37 degrees C) resulted in ce

283 ous ts alleles of spe-9, loss of function at nonpermissive temperatures is not due to protein misloca

284 formed growth-based selection experiments at nonpermissive temperatures using a library of random bet

285 layed a modestly increased Cse4 half-life at nonpermissive temperatures, suggesting that turnover of

286 At nonpermissive temperatures, they fail to splice, resulti

287 rently normal distribution at permissive and nonpermissive temperatures, yet mitosis appears to be ab

288 generate the TS phenotype at permissive and nonpermissive temperatures.

289 cally defective in Sir2-Sir4 interactions at nonpermissive temperatures.

290 itro, but only the rice isoforms denature at nonpermissive temperatures.

291 and the cellular signals in the surrounding nonpermissive tissue microenvironment that maintain the

292 lectively permissive environment, flanked by nonpermissive tissues.

293 ation and assembly, thereby rendering a cell nonpermissive to a specific class or species of viruses.

294 quiescent "bystander" CD4 T cells, which are nonpermissive to HIV infection, is a principal driver of

295 that fully assembled basement membranes are nonpermissive to smooth muscle cell (SMC) replication an

296 nous ligands, while other lipid ligands were nonpermissive to TCR binding.

297 strains carried the Xpr1(n) receptor variant nonpermissive to XMRV and xenotropic murine leukemia vir

298 Expression of hVRK1 during nonpermissive ts2 infections restored virus production a

299 the A30 and G7 proteins are unstable during nonpermissive tsH5 infections, suggesting that the loss

300 esistance to exogenous infection is due to a nonpermissive variant of the XPR1 gammaretrovirus recept